Phoney
Well-Known Member
That's how I always drink vodka!Alcohol was usually administered through a drip, but Dr Pillans said the hospital ran out so they had to feed Mr Lynam vodka through a nasal-gastric tube.
That's how I always drink vodka!Alcohol was usually administered through a drip, but Dr Pillans said the hospital ran out so they had to feed Mr Lynam vodka through a nasal-gastric tube.
You cloned, VB? Why on earth would you do that? That's a waste of tapwater!T.T.B.Co said:What a crock of ****. I am drinking a VB clone and im ok :icon_drunk:
Investigating the behaviour of methanol during the distillation it appears, that methanol is a companion of ethanol and therefore, by the possibilities of pot still distillation(2.3), rather hard to separate from ethanol. The investigation shows that there is in g/hl p.a. [pure alcohol] an increase of methanol contents during the distillation and especially in the last fractions (tailings). This is caused by the fact that methanol is, in spite of the lower boiling point (64,8°C) compared to ethanol (78,3°C), carried over in the distillate later than ethanol, an observation that is also confirmed by former investigations and in the literature.
The molecule structures however, show another aspect: ethanol has got one more CH2-group which makes the molecule less polar. So, concerning polarity, methanol can be ranged between water and ethanol and has therefore in the water phase a distillation behaviour different from ethanol. This may explain the behaviour which is rather contrary to the boiling points. This is no single appearance, because for example ethylacetate with a boiling point of 77°C, or, as an extreme case, is oamylacetate with 142°C are even carried over much earlier than methanol. Therefore methanol can not be separated using pot stills or normal column stills. Only special columns can separate methanol from the distillate(4.3).
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